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Data / Medical devices / United States / SAS Safety Corp.

SAS Safety Corp.: FDA-registered device maker in Cerritos, CA, United States, 1 510(k) clearance

SAS Safety Corp. is registered with the FDA (registration 2086655) in Cerritos, CA, United States. It lists 2 device types. The FDA files 1 510(k) clearance under its listings, the newest dated May 27, 2022. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
2086655
FEI number
3001695617
Address
17785 Center Court Dr N Ste 500, Cerritos, CA, United States, 90703
Owner or operator
SAS SAFETY CORP. (9033406)
Roles
Reprocessor
First device listed
July 25, 2022
Registered through
2026
Brand names listed
Astro Grip

Devices it lists

DeviceProduct codeClassRoleSource
Medical Glove, SpecialtyLZC1Reprocessoraccessdata.fda.gov
Polymer Patient Examination GloveLZA1Reprocessoraccessdata.fda.gov

510(k) clearances

The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.

Decided510(k) numberDeviceProduct codeDecisionApplicantSource
May 27, 2022K220609Powder-Free Nitrile Examination Glove Tested for Use with Chemotherapy Drugs and Fentanyl (White, Blue, Black, Orange and Green Color)LZASubstantially EquivalentEncompass Industries Sdn. Bhd.accessdata.fda.gov

Compare with other makers

Updated May 27, 2022. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.